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Sternberg Retractor

EUDAMED

Class I (EU MDR)

Ref 1008-13

by Dental Expert

Identity

Trade Name
STERNBERG RETRACTOR EUDAMED
Device Name
STERNBERG RETRACTOR EUDAMED
Model / Reference
1008-13 EUDAMED

Identifiers

Primary DI / UDI-DI
D1231008130 EUDAMED
Basic UDI-DI
++D123100813WA EUDAMED
EMDN Code
L03140105 SKIN RETRACTORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Sternberg Retractor by Dental Expert — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Dental Expert
EUDAMED SRN
PK-MF-000024595
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED 57134f37-0121-476a-b329-e00bbad05e65 61 fields · synced Jul 9, 2026